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排序方式: 共有447条查询结果,搜索用时 15 毫秒
91.
92.
A. L. Thompson R. G. Novy B. L. Farnsworth G. A. Secor N. C. Gudmestad J. R. Sowokinos E. T. Holm J. H. Lorenzen D. Preston 《American Journal of Potato Research》2005,82(6):481-488
Dakota Pearl (ND2676-10) is a medium-maturing chipping cultivar with uniform, round, bright white-skinned tubers with shallow eyes. Dakota Pearl has the ability to produce commercially acceptable chips following long-term storage at 5.5 C without the need for reconditioning. It yields well under both dryland and irrigated trial conditions in North Dakota. North Central Regional Potato Variety Trial and Snack Food Association Trial results indicate it has wide adaptability. Yield and specific gravity under dryland conditions are similar to Norchip; Dakota Pearl has a low percentage of external defects. Average set is 12 to 14 tubers per hill. Dakota Pearl demonstrates wide consumer appeal as a tablestock cultivar due to attractive tuber appearance and bright-white skin. Sensory evaluation scores for baking, boiling, and microwaving are comparable to those of standard chip cvs Atlantic, NorValley, and Snowden. The specific gravity of Dakota Pearl is similar to cvs Norchip and NorValley, lower than for Atlantic or Snowden. Total glycoalkaloid levels are low, at 1.5 mg/100 g fresh tuber tissue. The North Dakota Agricultural Experiment Station released Dakota Pearl on 23 April 1999. 相似文献
93.
VC McIver AS Tsang NE Symonds NR Perkins E Uquillas CM Dart LB Jeffcott AJ Dart 《Australian veterinary journal》2020,98(6):250-255
94.
R Akter AW Stent FM Sansom JR Gilkerson C Burden JM Devlin AR Legione CM El-Hage 《Australian veterinary journal》2020,98(11):570-573
Chlamydia psittaci was detected by PCR in the lung and equine foetal membranes of two aborted equine foetuses and one weak foal from two different studs in Victoria, Australia. The abortions occurred in September 2019 in two mares sharing a paddock northeast of Melbourne. The weak foal was born in October 2019 in a similar geographical region and died soon after birth despite receiving veterinary care. The detection of C. psittaci DNA in the lung and equine foetal membranes of the aborted or weak foals and the absence of any other factors that are commonly associated with abortion or neonatal death suggest that this pathogen may be the cause of the reproductive loss. The detection of C. psittaci in these cases is consistent with the recent detection of C. psittaci in association with equine abortion in New South Wales. These cases in Victoria show that C. psittaci, and the zoonotic risk it poses, should be considered in association with equine reproductive loss in other areas of Australia. 相似文献
95.
96.
A modified AACC 45‐g flour cookie procedure using asymmetrical centrifuge mixing as a replacement for conventional mixing has been developed. Ingredients are added to a pin cup in the same proportion as in the Approved Method 10‐50D (AACC 2000) sugar‐snap cookie test and mixed in a single step for 15 sec at 2,500 rpm. The dough is then processed and the resulting cookies are scored according to the AACC Approved Method 10–52 40‐g flour micro cookie test method. Cookies produced from a control cookie flour and four commercial soft wheat flours with the new mixing method did not show the characteristic surface cracking patterns normally obtained with conventional three‐stage mixing. However, with the exception of one spread value, no significant differences in spread, thickness, or the ratio of spread to thickness were evident when results were compared with those obtained with the AACC Approved Method 10‐50D 225‐g flour test method using a Hobart mixer equipped with a paddle. Cookies produced from two sets of advanced soft white spring wheat breeder lines, including control cultivars, using the asymmetrical centrifuge mixing procedure were also very comparable in spread, thickness, and ratio compared with those produced using 225 g of flour in the AACC Approved Method. Reproducibility of test results for all cookie parameters for both commercial and advanced plant breeder samples were comparable to the AACC Approved Method 10‐50D 225‐g flour test method. The very short mixing time and the ability to quickly clean or use multiple pin cups should allow very high throughput of flour samples relative to the use of conventional mixers for cookie testing. 相似文献
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98.
- 1. The freshwater pearl mussel Margaritifera margaritifera L. is globally endangered and is threatened by commercial exploitation, pollution and habitat loss throughout its range. Captive breeding would be a valuable tool in enhancing the status of M. margaritifera in the UK.
- 2. We have developed a semi‐natural system for successfully infecting juvenile brown trout with glochidial M. margaritifera, and culturing juvenile mussels in experimental tanks where glochidial M. margaritifera can excyst from fish gills and settle into sediment.
- 3. Infected fish had less than 1% mortality. Levels of infection varied among fish. Two yearly cohorts of juvenile M. margaritifera were identified from samples of sediment taken from each experimental tank. Individuals range in size from 1.4 mm (2000 cohort) to >3 mm in length (1999 cohort).
- 4. The number of juvenile M. margaritifera present in the two experimental tanks are estimated to be between 3600 (tank A) and 0 (tank B) for the putative 1999 cohort and between 6000 (tank A) and 13 000 (tank B) for the putative 2000 cohort.
- 5. This pioneering method for large‐scale cultivation of juvenile M. margaritifera is intermediate between the release of infected fish into rivers and the intensive cultivation systems developed in continental Europe and the USA for other species of unionid. This is the first time that large numbers of M. margaritifera have been cultured and represents a significant breakthrough in the conservation of this globally endangered Red Data List species. The method is straightforward and is most cost‐effective when undertaken alongside established hatchery processes.
99.
100.
Five steam-flaked sorghum grain (SFSG) samples with bulk densities of 476, 412, 347, 309 and 283 g/liter made by adjusting tension between mill rollers and three reconstituted sorghum grain (RSG) samples with reconstitution times of 10, 20 and 30 d and a control sample were analyzed for gas production kinetics (rumen liquor fermentation) and enzymatic glucose release (amyloglucosidase). Protein degradation was estimated from 6-h gas production and residual ammonia in the liquid. Gas production followed first-order kinetics (r2 greater than .98; P less than .01) and was used to describe rate and extent of digestion kinetics. Rate of gas production increased as processing degree increased. The magnitude of increase in gas production, however, was much less for RSG than for SFSG. Linear relationships were observed between enzymatic glucose release and the gas production rate constant k as well as gas production at 4,6 and 8 h (r2 greater than .98; P less than .01). Protein degradation decreased with processing degree of SFSG but increased with reconstitution time. A technique based on 6-h gas production and residual ammonia in the liquid is proposed to estimate both ruminal starch availability and ruminal protein degradability for processed sorghum grain. 相似文献